JP2015500832A - Medical food for meal management of depression and anxiety and its method - Google Patents
Medical food for meal management of depression and anxiety and its method Download PDFInfo
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- JP2015500832A JP2015500832A JP2014545850A JP2014545850A JP2015500832A JP 2015500832 A JP2015500832 A JP 2015500832A JP 2014545850 A JP2014545850 A JP 2014545850A JP 2014545850 A JP2014545850 A JP 2014545850A JP 2015500832 A JP2015500832 A JP 2015500832A
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Classifications
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/30—Dietetic or nutritional methods, e.g. for losing weight
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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Abstract
本発明は、0.0002mol%〜0.0278mol%のアイソトポログHOD、好ましくは0.0178mol%〜0.0278mol%のアイソトポログHODを含有する水を含む、うつ病及び/又は不安症の食事管理用医療食品に関する。さらに、本発明は、本発明の医療食品を、それを必要とする被検体に投与する工程を含む、うつ病及び/又は不安症の食事管理の方法に関する。さらに、本発明は、抗うつ薬を被検体に投与する工程と、本発明の医療食品を被検体に投与する工程とを含む、うつ病の治療方法に関する。さらに、本発明は、抗不安薬を被検体に投与する工程と、本発明の医療食品を被検体に投与する工程とを含む、不安症の治療方法に関する。【選択図】なしThe present invention relates to a dietary management medicine for depression and / or anxiety, comprising water containing 0.0002 mol% to 0.0278 mol% isotopologue HOD, preferably 0.0178 mol% to 0.0278 mol% isotopologue HOD. Regarding food. Furthermore, the present invention relates to a method for dietary management of depression and / or anxiety, comprising the step of administering the medical food of the present invention to a subject in need thereof. Furthermore, the present invention relates to a method for treating depression, comprising a step of administering an antidepressant to a subject and a step of administering the medical food of the present invention to the subject. Furthermore, the present invention relates to a method for treating anxiety, comprising a step of administering an anxiolytic drug to a subject and a step of administering the medical food of the present invention to the subject. [Selection figure] None
Description
本発明は、食品産業及び健康管理の分野に属する。より具体的には、本発明はうつ病及び不安症の食事管理用医療食品に関する。 The present invention belongs to the fields of food industry and health care. More specifically, the present invention relates to a medical food for dietary management of depression and anxiety.
うつ病は、気分の低下、活力の喪失、興味の喪失、身体的疾患を伴っている感覚(feelingof physical illness)、集中力の低下、食欲の変化、睡眠の変化、並びに身体機能及び精神機能の減退等の症状の組合せを特徴とし、容赦ない絶望感、無力感、罪悪感、及び不安感をもたらす障害である。世界的に、うつ病は能力低下及び早世の主な原因である。うつ病の正確な原因は不明である。現在のうつ病治療は、心理療法、抗うつ薬、又は両者の併用で構成される。しかしながら、うつ病障害の患者の食事管理に関連する特別な栄養要件は存在しない。 Depression is a decrease in mood, loss of vitality, loss of interest, feelings of physical illness, loss of concentration, changes in appetite, changes in sleep, and changes in physical and mental functions. It is characterized by a combination of symptoms such as decline, and is a disorder that causes unrelenting despair, helplessness, guilt and anxiety. Worldwide, depression is a major cause of disability and early life. The exact cause of depression is unknown. Current depression treatment consists of psychotherapy, antidepressants, or a combination of both. However, there are no special nutritional requirements related to dietary management for patients with depression disorders.
また、多くのうつ病は不安症を伴う。大うつ病患者の85%までが、全般性不安障害とも診断された。不安症は、恐怖、パニック、又は殆どの人が不安を感じないか若しくは脅かされていると感じない状況での不安等の症状の組合せを特徴とする障害である。不安症とうつ病は関係している。うつ病と不安症はいずれもストレスに対する生理的反応であり、共通の分子機構を共有する。現在の不安症の治療は、抗不安薬で構成される。しかしながら、不安障害の患者の食事管理に関連する特別な栄養要件は存在しない。 Many depressions are also accompanied by anxiety. Up to 85% of patients with major depression were also diagnosed with generalized anxiety disorder. Anxiety is a disorder characterized by a combination of symptoms such as fear, panic, or anxiety in situations where most people do not feel anxiety or threatened. Anxiety and depression are related. Depression and anxiety are both physiological responses to stress and share a common molecular mechanism. Current treatments for anxiety consist of anti-anxiety drugs. However, there are no special nutritional requirements related to dietary management for patients with anxiety disorders.
水は必須栄養素である。総水分摂取量は、飲料水、飲料中の水、及び食品に含有される水を含む。適切な総水分摂取量は、米国の調査データからの総水分摂取量の中央値に基づいて、男性及び女性それぞれ1日当たり3.7リットル及び2.7リットルと設定された(非特許文献1)。天然水は、安定な水素(H及びD)及び酸素(16O、17O、18O)の同位体により形成される9種の水アイソトポログ(H2 16O、H2 17O、H2 18O、H16OD、H17OD、H18OD、D2 16O、D2 17O、D18O)の組成物であり、主な水アイソトポログH2O(H2 16O)の含有量は99.7317分子%(mol%)であり、主な重水素含有アイソトポログHOD(H16OD)は0.0311mol%(国際標準水試料(Vienna Standard Mean Ocean Water:VSMOW))である(非特許文献2、非特許文献3)。海水の蒸発及び濃縮のプロセスのため、天然水のHODレベルは地球上の地域によってわずかに変化する。唯一除外されるのは南極大陸の天然水であり、約0.0178mol%のレベルでHODを含有する(Standard LightAntarctic Precipitation:SLAP)。多くの人々は、0.0280mol%〜0.0311mol%のHODレベルの天然水を消費する地球上の地域に居住する。計算基準により、1日当たり2.7リットル及び3.7リットルの天然水を消費する場合、女性及び男性は、それぞれ1日当たり絶対栄養素(obligate nutrient)として0.8ml以上及び1.0ml以上のHODを消費する。 Water is an essential nutrient. The total water intake includes drinking water, water in the beverage, and water contained in the food. Appropriate total water intake was set at 3.7 and 2.7 liters per day for males and females, respectively, based on the median total water intake from US survey data (Non-Patent Document 1). . Natural water consists of nine water isotopologues (H 2 16 O, H 2 17 O, H 2 18 ) formed by stable hydrogen (H and D) and oxygen ( 16 O, 17 O, 18 O) isotopes. O, H 16 OD, H 17 OD, H 18 OD, D 2 16 O, D 2 17 O, D 18 O) and the content of main water isotopologue H 2 O (H 2 16 O) Is 99.7317 molecule% (mol%), and the main deuterium-containing isotopologue HOD (H 16 OD) is 0.0311 mol% (International Standard Water Sample (Vienna Standard Mean Ocean Water: VSMOW)). Document 2, Non-Patent Document 3). Due to the process of seawater evaporation and concentration, the HOD level of natural water varies slightly from region to region. The only excluded is natural water from Antarctica, which contains HOD at a level of about 0.0178 mol% (Standard Light Antarctic Precipitation: SLAP). Many people live in areas on the planet that consume natural water with a HOD level of 0.0280 mol% to 0.0311 mol%. According to the calculation standard, when 2.7 liters and 3.7 liters of natural water are consumed per day, women and men each have an HOD of 0.8 ml or more and 1.0 ml or more as absolute nutrients per day. Consume.
本発明者らは、HODはうつ病及び不安症のもとでは非常に望ましくない栄養素であり、HODの制限が特別な医学的に決定された栄養素要件を表す可能性があり、その食事管理は通常の食事の修正のみでは達成され得ないことを見出した。驚くべきことに、本発明者らは、哺乳動物は飲料水中のHODレベルに非常に敏感であり、その天然濃度の範囲内で0.0006mol%のHOD含有量の変化でさえも心理的ストレスに対する感受性、並びに不安症及びうつ病の発症の素因に著しい影響をもたらすことを見出した。よって、うつ病及び/又は不安症の食事管理は、HODの1日消費量の制限によって達成され得る。 We have found that HOD is a highly undesirable nutrient under depression and anxiety, and the limitation of HOD may represent a special medically determined nutrient requirement, and its dietary management is It has been found that it cannot be achieved with only regular dietary modifications. Surprisingly, the inventors have found that mammals are very sensitive to HOD levels in drinking water, and even with a change in HOD content of 0.0006 mol% within its natural concentration range, it is sensitive to psychological stress. It has been found to have a significant impact on susceptibility and the predisposition to the development of anxiety and depression. Thus, dietary management of depression and / or anxiety can be achieved by limiting the daily consumption of HOD.
本発明の一目的は、0.0002分子%〜0.0278分子%のアイソトポログHODを含有する水を含む、うつ病及び/又は不安症の食事管理用医療食品を提供することである。 One object of the present invention is to provide a medical food for depression and / or anxiety diet management comprising water containing 0.0002 molecule% to 0.0278 molecule% isotopologue HOD.
本発明の一目的は、本発明の医療食品を、それを必要とする被検体に投与する工程を含む、うつ病及び/又は不安症の食事管理の方法を提供することである。 One object of the present invention is to provide a method for dietary management of depression and / or anxiety, comprising the step of administering the medical food of the present invention to a subject in need thereof.
本発明の一目的は、(a)抗うつ薬を被検体に投与する工程と、(b)本発明の医療食品を被検体に投与する工程とを含む、それを必要とする被検体におけるうつ病の治療方法を提供することである。 One object of the present invention includes (a) a step of administering an antidepressant to a subject, and (b) a step of administering the medical food of the present invention to the subject, in a subject in need thereof. It is to provide a method for treating disease.
本発明の一目的は、(a)抗不安薬を被検体に投与する工程と、(b)本発明の医療食品を被検体に投与する工程とを含む、それを必要とする被検体における不安症の治療方法を提供することである。 One object of the present invention includes (a) administering an anxiolytic drug to a subject and (b) administering the medical food of the present invention to the subject, and anxiety in the subject in need thereof. It is to provide a method for treating the disease.
本発明は、0.0002分子%〜0.0278分子%のアイソトポログHODを含有する水を含む、うつ病及び/又は不安症の食事管理用医療食品を提供する。 The present invention provides a dietary management medical food for depression and / or anxiety, comprising water containing 0.0002 molecule% to 0.0278 molecule% isotopologue HOD.
本発明の好ましい実施形態では、医療食品が0.0178分子%〜0.0278分子%のアイソトポログHODを含有する水を含む。 In a preferred embodiment of the present invention, the medical food product comprises water containing 0.0178 molecule% to 0.0278 molecule% isotopologue HOD.
本明細書で使用される「医療食品」の用語は、医師の管理下で経腸的に消費又は投与されるように製剤化された食品を指し、うつ病及び/又は不安症の具体的な食事管理を提供することが意図され、認識される科学原理に基づき、医学的評価によって特有の栄養要件が確立される食品を指す。 As used herein, the term “medical food” refers to food formulated to be consumed or administered enterally under the supervision of a physician, and is specific to depression and / or anxiety. Refers to foods that are intended to provide dietary management and for which specific nutritional requirements are established by medical assessment, based on recognized scientific principles.
本発明の好ましい実施形態では、医療食品は、特別に製剤化され、飲料製品として加工される。かかる飲料製品として、飲料水、飲料及び液体食品が挙げられるが、これらに限定されない。 In a preferred embodiment of the invention, the medical food is specially formulated and processed as a beverage product. Such beverage products include, but are not limited to, drinking water, beverages and liquid foods.
本明細書で使用される「うつ病」の用語は、典型的には、悲しい気分が続く及び/又は殆どの活動における興味若しくは喜びの喪失を特徴とする精神障害を指す。うつ病障害の例として、大うつ病としても知られる大うつ病障害、単極性障害、又は臨床的うつ病、大うつ病エピソード、非定型うつ病、(気分の)落ち込み、メランコリーうつ病、精神病性うつ病、高齢者のうつ病、心理社会的ストレス関連うつ病、及び産後うつ病が挙げられるが、これらに限定されない。 The term “depression” as used herein refers to a mental disorder that is typically characterized by a persistent sad mood and / or loss of interest or pleasure in most activities. Examples of depression disorders include major depression disorder, also known as major depression, unipolar disorder, or clinical depression, major depression episode, atypical depression, (mood) depression, melancholic depression, psychosis Examples include, but are not limited to, sexual depression, elderly depression, psychosocial stress-related depression, and postpartum depression.
本明細書で使用される「不安症」の用語は、不安障害又は不安な状態を指す。不安障害の例として、パニック発作、広場恐怖症、急性ストレス障害、特定の恐怖症、パニック障害、精神作用物質不安障害、器質性不安障害、強迫性不安障害、心的外傷後ストレス障害、全般性不安障害、及び特定不能の不安障害が挙げられるが、これらに限定されない。 As used herein, the term “anxiety” refers to an anxiety disorder or state of anxiety. Examples of anxiety disorders include panic attacks, agoraphobia, acute stress disorder, specific phobias, panic disorder, psychoactive substance anxiety disorder, organic anxiety disorder, obsessive compulsive anxiety disorder, posttraumatic stress disorder, generality Anxiety disorders and unspecified anxiety disorders include, but are not limited to.
本明細書で使用される「アイソトポログ」の用語は、IUPACCompendium of Chemical Terminology 第2版(1997)に従い、同位体組成(同位体置換の数)のみが異なる分子実態を指す。かかるアイソトポログの例として、H2 16O、H2 17O、H2 18O、H16OD、H17OD、1H18OD、D2 16O、D2 17O及びD2 18Oが挙げられる。本発明において、アイソトポログH16ODがHODとして表示される。 As used herein, the term “isotopologue” refers to molecular entities that differ only in isotopic composition (number of isotope substitutions) in accordance with IUPAC Compendium of Chemical Terminology, 2nd edition (1997). Examples of such isotopologues include H 2 16 O, H 2 17 O, H 2 18 O, H 16 OD, H 17 OD, 1 H 18 OD, D 2 16 O, D 2 17 O and D 2 18 O. It is done. In the present invention, isotopologue H 16 OD is displayed as HOD.
本発明の好ましい実施形態では、水中のHOD含有量を、当該技術分野からよく知られている方法により決定することができる。HODレベルは、レーザー分光法によって直接測定され得る(R.Van Trigt.R. van Trigt. Laser Spectrometry for Stable IsotopeAnalysis of Water Biomedical and PaleoclimatologicalApplications. 2002, Groningen: University Library Groningen)。また、HODレベルを、H/D比として従来の同位体質量分析法により決定し、水中の他の重水素含有アイソトポログの含有量がHODに比べて無視することができる程度であることを考慮して、HOD含有量に再度計算することができる。参照のため、VSMOW水は、0.00006mol%のH18OD、0.00001mol%のH17OD、並びに合計0.00001mol%未満のアイソトポログD2 16O、D2 17O及びD2 18Oを含有する。本発明の水における0.0002mol%〜0.0278mol%のアイソトポログHODの範囲は、重水素含有量1ppm〜139ppmの範囲に相当する。本発明の水における0.0178mol%〜0.0278mol%のアイソトポログHODの範囲は、重水素含有量89ppm〜139ppmの範囲に相当する。 In a preferred embodiment of the invention, the HOD content in water can be determined by methods well known from the art. HOD levels can be measured directly by laser spectroscopy (R. Van Trigt. R. van Trigt. Laser Spectrometry for Stable Isotope Analysis of Water Biomedical and Paleoclimatological Applications. 2002, Groningen: University Library Groningen). In addition, considering that the HOD level is determined by conventional isotope mass spectrometry as the H / D ratio, the content of other deuterium-containing isotopologues in water is negligible compared to HOD. The HOD content can be recalculated. For reference, VSMOW water contains 0.00006 mol% H 18 OD, 0.00001 mol% H 17 OD, and a total of less than 0.00001 mol% isotopologues D 2 16 O, D 2 17 O and D 2 18 O. contains. The range of 0.0002 mol% to 0.0278 mol% isotopologue HOD in the water of the present invention corresponds to the range of 1 ppm to 139 ppm of deuterium content. The range of 0.0178 mol% to 0.0278 mol% isotopologue HOD in the water of the present invention corresponds to the range of deuterium content 89 ppm to 139 ppm.
本発明の好ましい実施形態では、0.0002mol%〜0.0278mol%のアイソトポログHODを含有する水を、当該技術分野からよく知られている様々な工業的手法、例えば天然水の減圧蒸留により調製することができる。0.0178mol%〜0.0278mol%のアイソトポログHODを含有する水を希少な天然起源(例えば、南極地方の降水)から得ることができ、又は当該技術分野からよく知られている様々な工業的手法、例えば天然水の減圧蒸留により調製することができる。 In a preferred embodiment of the present invention, water containing 0.0002 mol% to 0.0278 mol% isotopologue HOD is prepared by various industrial techniques well known from the art such as vacuum distillation of natural water. be able to. Water containing 0.0178 mol% to 0.0278 mol% isotopologue HOD can be obtained from a rare natural source (eg, Antarctic precipitation), or various industrial techniques well known from the art For example, it can be prepared by distillation under reduced pressure of natural water.
本発明の実施においては、0.0002mol%〜0.0278mol%のアイソトポログHODを含有する水は、天然レベルと同等又はそれとは異なるレベル、例えば、0<H2 18O≦0.2000mol%、0<H2 17O≦0.0370mol%、0<H17OD≦0.0270mol%、0<H18OD≦0.0270mol%、0<D2 16O≦0.0270mol%、0<D2 17O≦0.0270mol%、及び0<D2 18O≦0.0270mol%で他の水アイソトポログを含有してもよい。 In the practice of the present invention, water containing 0.0002 mol% to 0.0278 mol% isotopologue HOD is at a level equivalent to or different from the natural level, for example, 0 <H 2 18 O ≦ 0.2000 mol%, 0 <H 2 17 O ≦ 0.0370 mol%, 0 <H 17 OD ≦ 0.0270 mol%, 0 <H 18 OD ≦ 0.0270 mol%, 0 <D 2 16 O ≦ 0.0270 mol%, 0 <D 2 17 Other water isotopologues may be included with O ≦ 0.0270 mol% and 0 <D 2 18 O ≦ 0.0270 mol%.
本発明の医療食品は、よく知られた任意の原料を使用するよく知られた手法によって調製され得る。かかる任意の原料は、一般的には組成物の約0.0005重量%〜約10.0重量%、好ましくは約0.005重量%〜約1.0重量%のレベルで個別に使用される。好適な任意の原料の例として、緩衝液、甘味料、着色剤、担体等が挙げられるが、これらに限定されない。 The medical food of the present invention can be prepared by a well-known technique using any well-known raw material. Such optional ingredients are generally used individually at a level of from about 0.0005% to about 10.0%, preferably from about 0.005% to about 1.0%, by weight of the composition. . Examples of suitable optional ingredients include, but are not limited to, buffers, sweeteners, colorants, carriers and the like.
本発明の好ましい実施形態では、医療食品は、飲料水又は飲料の形態で特別に製剤化され製造された液体医療食品である。液体医療食品は、0.0002mol%〜0.0279mol%のアイソトポログHODを含有する水を、二酸化炭素又は/及び典型的には天然飲料水に豊富な(abundant)無機塩で飽和することにより調製され得る。かかる塩の例として、塩化ナトリウム、重炭酸ナトリウム、塩化カルシウム、硫酸マグネシウム等が挙げられるが、これらに限定されない。 In a preferred embodiment of the invention, the medical food is a liquid medical food specially formulated and manufactured in the form of drinking water or beverage. Liquid medical foods are prepared by saturating water containing 0.0002 mol% to 0.0279 mol% isotopologue HOD with carbon dioxide or / and typically mineral water abundant. obtain. Examples of such salts include, but are not limited to sodium chloride, sodium bicarbonate, calcium chloride, magnesium sulfate and the like.
さらに、本発明は、本発明の医療食品を、それを必要とする被検体に投与する工程を含む、うつ病及び/又は不安症の食事管理の方法を提供する。 Furthermore, the present invention provides a method for dietary management of depression and / or anxiety, comprising the step of administering the medical food of the present invention to a subject in need thereof.
本発明の方法の実施においては、医療食品は、1日又はそれより長い期間に亘って、食事を管理し、及び/又は医学的管理を提供する医師によって処方された量で経口的に投与され得る。 In the practice of the method of the present invention, the medical food is administered orally in an amount prescribed by a physician who manages the diet and / or provides medical management over a period of one day or longer. obtain.
本発明の方法の実施においては、医療食品は、1日当たり被検体当たり0.1〜4.0リットルの量で投与することができる飲料水又は飲料として製剤化されてもよい。 In the practice of the method of the invention, the medical food may be formulated as drinking water or beverage that can be administered in an amount of 0.1-4.0 liters per subject per day.
さらに、本発明は、(a)抗うつ薬を被検体に投与する工程と、(b)本発明の医療食品を被検体に投与する工程とを含む、それを必要とする被検体におけるうつ病の治療方法を提供する。 Furthermore, the present invention includes (a) a step of administering an antidepressant to a subject, and (b) a step of administering the medical food of the present invention to the subject, and depression in a subject in need thereof. A method of treatment is provided.
本明細書で使用される「抗うつ薬」の用語は、うつ病を治療するために使用される薬剤を指す。かかる薬剤として、限定されることなく、クロミプラミン、アモキサピン、ノルトリプチリン、モプロチレン(moprotilene)、トリミプラミン、イミプラミン、又はプロトリプチリン等の三環系抗うつ薬、モノアミン酸化酵素阻害剤、シタロプラム、エスシタロプラム、デュロキセチン、フルオキセチン、セルトラリン、ノルセルトラリン、パロキセチン、ミルトラゼピン(mirtrazepine)、フルボキサミン、ミルナシプラン、クロミンプラミン(clominpramine)、フェモキセチン、インダプリン(indapline)、アラプロルクレート(alaprolclate)、セリクラミン、又はイフォキセチン等の選択的セロトニン再取り込み阻害剤を含むセロトニン再取り込み阻害剤、デシプラミン、マプロチリン、ロフェプラミン、レボキセチン、オキサプロチリン、フェゾラミン、トモキセチン、又は(S,S)−ヒドロキシブプロピオン等の選択的ノルエピネフリン再取り込み阻害剤を含むノルエピネフリン再取り込み阻害剤、アミネプチン、ブプロピオン、及びベンラファキシン等のドーパミン再取り込み阻害剤、並びにベンラファキシン、ネファゾドン、又はトラゾドン等の非定型抗うつ薬、上述のいずれかの治療的に活性なアイソマー又は代謝物、並びに上述のいずれか1つの薬学的に許容される塩、溶媒和物、クラスレート、多形体又は共結晶が挙げられる。 As used herein, the term “antidepressant” refers to an agent used to treat depression. Such drugs include, without limitation, tricyclic antidepressants such as clomipramine, amoxapine, nortriptyline, moprotilene, trimipramine, imipramine, or protriptyline, monoamine oxidase inhibitors, citalopram, escitalopram, duloxetine, Reselective celloselectives such as fluoxetine, sertraline, norsertraline, paroxetine, mirtrazepine, fluvoxamine, milnacipran, clominpramine, femoxetine, indapline, alaprolclate, cerixamine, or ifoxetine Serotonin reuptake inhibitors, including inhibitors, desipramine, maprotiline, lofepramine, reboxetine, oxaprotilin, fezola , Tomoxetine, or a selective norepinephrine reuptake inhibitor such as (S, S) -hydroxybupropion, a norepinephrine reuptake inhibitor, a dopamine reuptake inhibitor such as amineptin, bupropion, and venlafaxine, and venlafaxine Atypical antidepressants such as nefazodone or trazodone, any of the above therapeutically active isomers or metabolites, and any one of the above pharmaceutically acceptable salts, solvates, clathrates, Polymorphs or co-crystals are mentioned.
本発明の方法の実施においては、医師によって処方されたように抗うつ薬を投与する。 In practicing the method of the invention, an antidepressant is administered as prescribed by a physician.
さらに、本発明は、(a)抗不安薬を被検体に投与する工程と、(b)本発明の医療食品を被検体に投与する工程とを含む、それを必要とする被検体における不安症の治療方法を提供する。 Furthermore, the present invention comprises (a) a step of administering an anxiolytic drug to a subject, and (b) a step of administering the medical food of the present invention to the subject, wherein the anxiety in the subject in need thereof A method of treatment is provided.
本明細書で使用される「抗不安薬」の用語は、不安症を治療するために使用される薬剤を指す。かかる薬剤として、限定されることなく、クロナゼパム、アルプラゾラム、ロラゼパム、クロラゼペート、オキサゼパム、フルラゼパム、ジアゼパム、ハラゼパム、プラゼパム、クロルジアゼポキシド、ブスピロン、ゲピロン、タンドスピロン、イプサピロン、ベンタゼパム、シタロプラム、クロバザム、クロチアゼパム、エチホキシン、エチゾラム、デロラゼパム、ロフラゼプ酸エチル、フルタゾラム、フルオキセチン、フルトプラゼパム、ケタゾラム、メタクラゼパム、メキサゾラム、モクロベミド、オキサゾラム、トフィソパム、ピナゼパム、パロキセチン、ピバガビン、リルマザホン、セルトラリン、チアネプチン、ベンラファキシン、ゾテピン、エスシタロプラム、フルボキサミン、プレガバリン、アゴメラチン、デュロキセチン、オシナプロン、パゴクロン、アプレピタント、デクスメデトミジン、エグルメガド、エプリバンセリン、ベスチピタント、レベチラセタム、オランザピン、チアガビン、エマプニル(emapunil)、デキストフィソパム(dextofisopam)、イトリグルミド、S−デスメチルゾピクロン、ガバペンチン、オピプラモール、スマトリプタン、及びネファゾドン、上述のいずれかの治療的に活性なアイソマー又は代謝物、並びに上述のいずれか1つの薬学的に許容される塩、溶媒和物、クラスレート、多形体、又は共結晶が挙げられる。 As used herein, the term “anti-anxiety drug” refers to an agent used to treat anxiety. Such drugs include, but are not limited to, clonazepam, alprazolam, lorazepam, chlorazepate, oxazepam, flurazepam, diazepam, halazepam, prazepam, chlordiazepoxide, buspirone, gepirone, tandospirone, ipsapilone, bentazepam throxam, citalopram Delorazepam, ethyl loflazepate, flutazolam, fluoxetine, furtoprazepam, ketazolam, methaclazepam, mexazolam, moclobemide, oxazolam, tofisopam, pinazepam, paroxetine, pivagabine, rilazaphone, sertraline, thiantazomine, venlafaxine, venlafaxine Duloxetine Oninapron, Pagoclone, Aprepitant, Dexmedetomidine, Egourandad, Eprivanserin, Bestipitant, Levetiracetam, Olanzapine, Thiagabine, Emapnil (emapunil), Dextofisopam, Itriglumide, S-desmethylzopicanthropam Nefazodone, any of the above-mentioned therapeutically active isomers or metabolites, and any one of the above-mentioned pharmaceutically acceptable salts, solvates, clathrates, polymorphs, or co-crystals.
本発明の方法の実施においては、医師によって処方されたように抗不安薬を投与する。 In practicing the method of the invention, an anxiolytic is administered as prescribed by a physician.
本明細書で使用される「被検体」の用語は、任意の哺乳動物を指す。かかる哺乳動物の包括的な例として、イヌ、ネコ、ウマ及びヒト等の動物が挙げられるが、これらに限定されない。好ましくは、被検体はヒトである。 As used herein, the term “subject” refers to any mammal. Comprehensive examples of such mammals include, but are not limited to, animals such as dogs, cats, horses and humans. Preferably, the subject is a human.
本発明を立証するため以下の実施例を提示する。実施例は解説であるにすぎず、本発明の範囲を何ら限定することを意図するものではない。 The following examples are presented to demonstrate the invention. The examples are illustrative only and are not intended to limit the scope of the invention in any way.
実施例1
表1は、本発明の医療食品を調製するための0.0002分子%〜0.0278分子%のアイソトポログHODを含む水試料を示す。或る特定の割合で対照天然水(0.0300mol%HOD)と、60℃及び0.2barの気圧での減圧蒸留により調製された水(0.0178mol%HOD)とを混合することにより、天然濃度0.0178mol%〜0.0278mol%の範囲内でアイソトポログHODを含有する水の試料を調製した。60℃及び0.2barの気圧での天然水の長期減圧蒸留により、0.0002mol%〜0.0278mol%の範囲内でアイソトポログHODを含有する水の試料を調製した。HODレベルを同位体レーザー分光法により測定した。
Example 1
Table 1 shows a water sample containing 0.0002 molecule% to 0.0278 molecule% isotopologue HOD for preparing the medical food of the present invention. By mixing control natural water (0.0300 mol% HOD) in a certain proportion with water (0.0178 mol% HOD) prepared by vacuum distillation at 60 ° C. and 0.2 bar pressure. A sample of water containing isotopologue HOD was prepared in a concentration range of 0.0178 mol% to 0.0278 mol%. A sample of water containing isotopologue HOD was prepared in the range of 0.0002 mol% to 0.0278 mol% by long-term vacuum distillation of natural water at 60 ° C. and a pressure of 0.2 bar. HOD levels were measured by isotope laser spectroscopy.
実施例2
表2は、うつ病及び不安症の食事管理用医療食品を示す。
Example 2
Table 2 shows medical foods for dietary management of depression and anxiety.
塩化カルシウム、塩化マグネシウム、及び重炭酸ナトリウムを室温下で水に溶解し、その後、得られた生成物を330mlの容量のビンに詰めた。 Calcium chloride, magnesium chloride, and sodium bicarbonate were dissolved in water at room temperature and the resulting product was then packaged in 330 ml capacity bottles.
実施例3
本実施例は、HODがうつ病を発症させやすくする飲料水中の望ましくない絶対栄養素であることを立証する。HODのうつ病様行動の素因(predisposing)に対する影響を強制水泳試験(FST)において評価した。個別に飼育された若年成体雄C57Bl/6マウスを各群n=12で使用した。マウスは、2週間に亘り飲料水として自由に実施例1のNo1〜No4の水試料を受け、24時間間隔で2セッションのFSTにおいて試験した。環境温度の水で水位13cm(シリンダーの縁まで7cm)まで満たした直径17cmのガラスシリンダーにおいて、強制水泳試験を行った。動物を6分間採点した。FSTでは、マウスは浮遊期間の増加によりうつ病様行動を示す。2回目のFSTセッションでの浮遊期間をうつ病様行動の基準とした。post−hoc解析としてANOVA及びMann−Whitney検定を使用し、統計学的解析を行った。浮遊期間の平均±SEMとしてデータを表3に提示する。
Example 3
This example demonstrates that HOD is an undesired absolute nutrient in drinking water that predisposes to depression. The effect of HOD on the predisposing of depression-like behavior was evaluated in the forced swimming test (FST). Individual adult male C57B1 / 6 mice were used for each group n = 12. Mice received the water samples of No. 1 to No. 4 of Example 1 freely as drinking water for 2 weeks and were tested in 2 sessions of FST at 24 hour intervals. The forced swimming test was performed in a glass cylinder with a diameter of 17 cm filled with water at ambient temperature to a water level of 13 cm (7 cm to the edge of the cylinder). Animals were scored for 6 minutes. In FST, mice exhibit depression-like behavior by increasing the floating period. The floating period in the second FST session was used as a standard for depression-like behavior. Statistical analysis was performed using ANOVA and Mann-Whitney test as post-hoc analysis. Data are presented in Table 3 as mean ± SEM of the floating period.
これらの結果は、うつ病の素因が飲料水中のHODレベルに依存することを示唆している。よって、HODはうつ病のもとでは非常に望ましくない栄養素であり、HODの制限が特別な医学的に決定された栄養素要件を表す可能性があり、その食事管理は通常の食事の修正のみでは達成され得ない。 These results suggest that the predisposition to depression depends on the HOD level in the drinking water. Thus, HOD is a highly undesirable nutrient under depression and HOD restrictions may represent special medically determined nutrient requirements, and its dietary management is not limited to normal dietary modifications alone Cannot be achieved.
実施例4
本実施例は、HODが、うつ病の中核症状である無快感症を発症させやすくする飲料水中の望ましくない栄養素であることを立証する。無快感症の素因に対するHODの影響を、慢性ストレスモデルの齧歯動物において評価した。個別に飼育された若年成体雄CD1マウスを各群n=20で使用した。ストレス開始前の1週間及び10日間のストレスの間に亘って、マウスは飲料水として自由に実施例1の水試料No1〜No4を受けた。ストレス処理の10日目において、スクロース選択について動物を試験した。スクロース選択試験では、マウスはスクロース選択の低下によりうつ病様行動の中核症状である無快感症を示す。post−hoc解析としてANOVA及びMann−Whitney検定を使用して、統計学的解析を行った。スクロース選択の割合を平均±SEMとして、データを表4に提示する。
Example 4
This example demonstrates that HOD is an undesirable nutrient in drinking water that facilitates the development of anxiety, a core symptom of depression. The effect of HOD on predisposition to anorexia was evaluated in rodents in a chronic stress model. Individual adult male CD1 mice were used in each group n = 20. During the 1 week and 10 days of stress prior to the start of stress, the mice received the water samples No1-No4 of Example 1 freely as drinking water. On day 10 of stress treatment, animals were tested for sucrose selection. In the sucrose selection test, mice exhibit annoyance, a core symptom of depression-like behavior, due to reduced sucrose selection. Statistical analysis was performed using ANOVA and Mann-Whitney test as post-hoc analysis. Data are presented in Table 4 with the percentage of sucrose selection as mean ± SEM.
*ストレス負荷対照と有意に異なる(P<0.05)
* Significantly different from stress load control (P <0.05)
これらの結果は、うつ病の中核症状である無快感症の素因は飲料水中のHODレベルに依存することを示唆している。よって、HODはうつ病のもとでは非常に望ましくない栄養素であり、HODの制限が特別な医学的に決定された栄養素要件を表す可能性があり、その食事管理は通常の食事の修正のみでは達成され得ない。 These results suggest that the predisposition to anorexia, the core symptom of depression, depends on the HOD level in the drinking water. Thus, HOD is a highly undesirable nutrient under depression and HOD restrictions may represent special medically determined nutrient requirements, and its dietary management is not limited to normal dietary modifications alone Cannot be achieved.
実施例5
本実施例は、HODが不安症を発症させやすくする飲料水中の望ましくない栄養素であることを立証する。不安症の素因に対するHODの影響を、齧歯動物において0字型迷路試験で評価した。個別に飼育された若年成体雄C57Bl/6マウスを各群n=12で使用した。マウスは、2週間に亘って自由に飲料水として実施例1の水試料No1〜No4を受け、0字型迷路試験において試験した。0字型迷路試験では、マウスは迷路の壁のない走行部(open arms)の回避により不安を示す。壁のない走行部における経過時間を不安行動の基準とした。post−hoc解析としてANOVA及びMann−Whitney検定を使用して、統計学的解析を行った。壁のない走行部における経過時間の平均±SEMとして、データを表5に提示する。
Example 5
This example demonstrates that HOD is an undesired nutrient in drinking water that predisposes to developing anxiety. The effect of HOD on predisposition to anxiety was assessed in rodents with a zero-shaped maze test. Individual adult male C57B1 / 6 mice were used for each group n = 12. Mice received the water samples No1-No4 of Example 1 as drinking water freely over 2 weeks and tested in a 0-shaped maze test. In the 0-shaped maze test, the mice are anxious by avoiding the open arms without the maze walls. The elapsed time in the running section without a wall was used as the standard for anxiety behavior. Statistical analysis was performed using ANOVA and Mann-Whitney test as post-hoc analysis. The data is presented in Table 5 as the mean ± SEM of elapsed time in the running section without walls.
これらの結果は、不安症の素因が飲料水中のHODレベルに依存することを示唆している。よって、HODは不安症のもとでは非常に望ましくない栄養素であり、HODの制限が特別な医学的に決定された栄養素要件を表す可能性があり、その食事管理は通常の食事の修正のみでは達成され得ない。 These results suggest that the predisposition to anxiety depends on the HOD level in the drinking water. Thus, HOD is a highly undesirable nutrient under anxiety, and restrictions on HOD may represent special medically determined nutrient requirements, and dietary management is not limited to normal dietary modifications alone Cannot be achieved.
実施例6
本実施例は、うつ病の治療方法を立証する。強制水泳試験(FST)における経口で6mg/kgの抗うつ薬イミプラミンの効果を、FSTの前2週間に亘り、飲料水として自由に実施例2の対照食品又は医療食品No1を受けた成体雄C57Bl/6マウスにおいて評価した。FSTでは、マウスは浮遊待機時間の増加によりうつ病様行動を示す。FSTセッションでの浮遊待機時間を強制水泳行動の基準とした。post−hoc解析としてANOVA及びMann−Whitney検定を使用して、統計学的解析を行った。浮遊待機時間の平均±SEMとして、表6にデータを提示する。
Example 6
This example demonstrates a method for treating depression. The effect of 6 mg / kg of the antidepressant imipramine orally in the forced swimming test (FST) was compared to the adult male C57B1 who received the control food or medical food No1 of Example 2 freely as drinking water for 2 weeks before the FST. / 6 mice were evaluated. In FST, mice exhibit depression-like behavior by increasing the floating waiting time. The floating waiting time in the FST session was used as the standard for forced swimming behavior. Statistical analysis was performed using ANOVA and Mann-Whitney test as post-hoc analysis. Data are presented in Table 6 as mean ± SEM of floating waiting time.
表6は、抗うつ薬によるうつ病の治療が、本発明の医療食品を用いたうつ病の食事管理と併用された場合に改善されることを立証している。 Table 6 demonstrates that the treatment of depression with antidepressants is improved when combined with the dietary management of depression with the medical food of the present invention.
実施例7
本実施例は、不安症の治療方法を立証する。抗不安薬ジアゼパム0.125mg/kgの皮下注射の0字型迷路試験における効果を、0字型迷路試験の前2週間に亘り、飲料水として自由に実施例2の対照食品又は医療食品No2を受けた成体雄C57Bl/6マウスにおいて評価した。0字型迷路試験では、マウスは迷路の壁のない走行路の回避により不安を示す。壁のない走行路における経過時間を不安行動の基準とした。post−hoc解析として、ANOVA及びMann−Whitney検定を使用し、統計学的解析を行った。壁のない走行路における経過時間の平均±SEMとして、表7にデータを提示する。
Example 7
This example demonstrates a method for treating anxiety. The effect of the anxiolytic diazepam 0.125 mg / kg subcutaneous injection in the 0-shaped maze test was freely used as drinking water for 2 weeks before the 0-shaped maze test. Evaluation was performed in adult male C57B1 / 6 mice. In the 0-shaped maze test, the mouse is anxious by avoiding a runway without a maze wall. The elapsed time on the road with no walls was used as the standard for anxiety behavior. Statistical analysis was performed using ANOVA and Mann-Whitney test as post-hoc analysis. The data is presented in Table 7 as the mean ± SEM of elapsed time on the road without walls.
表7は、抗不安薬による不安症の治療が、本発明の医療食品を用いた不安症の食事管理と併用された場合に改善されることを立証している。 Table 7 demonstrates that treatment of anxiety with anxiolytics is improved when combined with anxiety diet management using the medical food of the present invention.
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